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Genetic diversity of endangered Manglietia patungensis assessed by inter simple sequence repeat and sequence-related amplified polymorphism markers
Institution:1. Biotechnology Research Center, China Three Gorges University, Yichang, Hubei 443002, PR China;2. College of Forestry, Henan University of Science and Technology, Luoyang 471003, PR China;3. Key Laboratory for Silviculture and Conservation of the Ministry of Education, Beijing Forestry University, Beijing 100083, PR China;1. School of Computer Science and Technology, Shandong University, Jinan 250100, China;2. School of Mathematics, Shandong University, Jinan 250100, China;3. Department of Computer Science, Montana State University, Bozeman, MT 59717, USA;1. College of Life Sciences, Shaanxi Normal University, Xi''an 710062, China;2. National Engineering Laboratory for Resource Developing of Endangered Chinese Crude Drugs in Northwest of China, Xi''an, Shaanxi 710062, China;3. Meteorological Bureau of Shaanxi Province, Xi''an 710014, China;1. Department of Botany, Rhodes University, Grahamstown 6140, South Africa;2. Selmar Scholand Herbarium, Department of Botany, Rhodes University, Grahamstown 6140, South Africa;1. National Engineering Laboratory for Resource Developing of Endangered Chinese Crude Drugs in Northwest of China, College of Life Sciences, Shaanxi Normal University, Xi''an, 710062, China;2. Core Research Laboratory, the Second Affiliated Hospital, School of Medicine, Xi''an Jiaotong University, Xi''an, 710004, China;3. Climate Research Center, Meteorological Bureau of Shaanxi Province, Xi''an, 710014, China
Abstract:Manglietia patungensis Hu is an endangered plant native to China. Knowledge of its genetic diversity and structure would aid its conservation. This study assessed nine natural populations of M. patungensis using two methods: inter simple sequence repeat (ISSR) and sequence-related amplified polymorphism (SRAP) markers. Using 10 ISSR primer pairs, 334 bands were generated, and 10 SRAP primer pairs generated 276 bands. The percent of polymorphic bands (91.32% and 93.48%), Nei's genetic diversity (0.3448 and 0.3323), and Shannon's information index (0.5075 and 0.4935) revealed a high level of genetic diversity at the species level. Total heterozygosity was 0.3439 by ISSR and 0.3281 by SRAP. The mean heterozygosity was 0.2323 by ISSR and 0.2521 by SRAP. The coefficient of genetic differentiation among natural populations was 0.3245 by ISSR and 0.2316 by SRAP. These data indicated higher levels of genetic diversity of M. patungensis within, rather than among, populations. Estimates of gene flow among natural populations were 1.0411 and 1.0589, which implied a certain amount of gene exchange among populations. A Mantel test revealed no significant correlation between genetic and geographic distance. ISSR and SRAP markers are both effective for genetic diversity research in M. Patungensis. Based on these results, conservation of M. patungensis should be performed both in situ and ex situ.
Keywords:Genetic diversity  Genetic differentiation  ISSR  SRAP  conservation strategy
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